eudamed_udi
Primary ID: 08053847360433
FLOW CANNULA S with fixing for NIV/CPAP (UDI 08053847360433)
Manufactured by GINEVRI srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FLOW CANNULA S with fixing for NIV/CPAP - Primary ID 08053847360433
Device Regulatory Overview
The FLOW CANNULA S with fixing for NIV/CPAP (Model/Catalog Number: 13612H73) is a medical device manufactured by GINEVRI srl. This product is indexed under FDA Product Code / Category Classification V0502 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 13612H73
- Product Code / EMDN
- V0502
- Device Name
- FLOW CANNULA with fixing for NIV/CPAP
- Database Sync Date
- 2026-08-09 17:50:31
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of FLOW CANNULA S with fixing for NIV/CPAP?
The registered manufacturer of record for FLOW CANNULA S with fixing for NIV/CPAP is GINEVRI srl.
What is the Primary UDI-DI identifier for FLOW CANNULA S with fixing for NIV/CPAP?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08053847360433.
What classification code is assigned to this device?
This device is registered under product classification code V0502.
Similar Classification Devices (V0502)
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